KJA11200B

GUDID 00840085248344

OBLIQUE ALIF PLATE, ZERO

HYHTE HOLDINGS, INC.

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage
Primary Device ID00840085248344
NIH Device Record Keyded77be4-b2ef-4795-a391-4a4933c1f4f4
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberKJA11200B
Catalog NumberKJA11200B
Company DUNS073029645
Company NameHYHTE HOLDINGS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM

Device Dimensions

Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree
Height11 Millimeter
Angle15 degree

Device Identifiers

Device Issuing AgencyDevice ID
GS100840085248344 [Primary]

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


[00840085248344]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-16
Device Publish Date2022-05-06

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00840085265129 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265136 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265143 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265150 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085257469 - NA2024-04-18 DUAL LEAD SCREW
00840085257476 - NA2024-04-18 DUAL LEAD SCREW

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